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2-Iodo-3-Hydroxypyridine

    • Product Name 2-Iodo-3-Hydroxypyridine
    • Alias 2-Iodo-3-pyridinol
    • Einecs 810-210-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    314627

    Product Name 2-Iodo-3-Hydroxypyridine
    Cas Number 1120-79-6
    Molecular Formula C5H4INO
    Molecular Weight 221.00 g/mol
    Appearance Off-white to light brown solid
    Melting Point 88-92°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 2-Iodo-3-Hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Iodo-3-Hydroxypyridine is supplied in a 5-gram amber glass bottle with a secure screw cap and tamper-evident seal.
    Shipping 2-Iodo-3-Hydroxypyridine is securely packaged in sealed containers to prevent moisture and air exposure. It is shipped in compliance with all relevant chemical transport regulations, including proper labeling and documentation. During transit, it is handled as a hazardous chemical, ensuring safety for both personnel and the environment. Expedited shipping is available upon request.
    Storage 2-Iodo-3-Hydroxypyridine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Store at temperatures between 2–8°C (refrigerator), and ensure the storage area is properly labeled and equipped for chemical safety. Avoid moisture and ignition sources.
    Application of 2-Iodo-3-Hydroxypyridine

    Applications of 2-Iodo-3-Hydroxypyridine in Industrial Manufacturing

    2-Iodo-3-Hydroxypyridine serves as a strategic raw material across several advanced technical fields, particularly in pharmaceutical and agrochemical syntheses, due to its unique functional group arrangement and halogen reactivity. The following sections outline real and established industrial application scenarios, focusing on compliance, formulation guidance, integration in downstream processes, and the nature of resulting end products.

    1. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    Leading pharmaceutical manufacturers rely on 2-Iodo-3-Hydroxypyridine as a key intermediate during multi-step syntheses of pyridine-derived antivirals. Specialized process development teams optimize its use in regulated environments to facilitate halogen exchange and further derivatization, directly impacting the yield and regulatory standing of high-purity drug substances destined for stringent regulated markets.

    Industry compliance standards

    • ICH Q7 cGMP for Active Pharmaceutical Ingredients
    • EU Guidelines for Good Manufacturing Practice (EudraLex Volume 4)
    • USP <795>, <797> (as referenced for intermediates and laboratory controls)
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.12–0.35 molar equivalents relative to primary pyridine scaffold, adjusted based on targeted substitution and step yield during route optimization

    Downstream process integration

    • Reaction enters during nucleophilic substitution sequence, often at the second or third step after initial pyridine ring assembly, followed by halogen-metal exchange and functionalization for the designated API progression

    Final product types

    • Oseltamivir intermediates
    • Hepatitis B pyridone-based drugs
    • Novel pyridone-containing antiviral leads in clinical development

    2. Agrochemical Precursor in Fungicide Manufacture

    Manufacturers of active fungicidal ingredients utilize this material within the synthesis of pyridine-derived actives. Its specific iodine substitution enables the reliable construction of heterocyclic moieties required for targeted activity against fungal pathogens, providing consistent batch-to-batch control in line with international agrochemical standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC No 1907/2006) for chemical registration and evaluation
    • Chemical Facility Anti-Terrorism Standards (CFATS, US)
    • ISO 9001:2015 Quality Management in Agrochemical Processing

    Typical usage ratio

    • 0.18–0.28 mol/mol of the target heterocyclic building block, precise dosage established during scale-up and subject to raw material conversion efficiency

    Downstream process integration

    • Integrated as the halogenated pyridine input for the cyclization step, with subsequent catalytic modifications to build the bioactive ring system preferred in modern crop protection agents

    Final product types

    • Pyridone-based fungicide active ingredients (e.g., for rice and wheat protection)
    • Seed treatment formulation precursors
    • Preventive spray concentrate actives

    3. Diagnostic Reagent and Radiolabelled Tracer Synthesis

    In the diagnostic reagent field, contract manufacturers employ 2-Iodo-3-Hydroxypyridine as a precursor for radioiodination, supporting the production of labeled tracers for imaging and research. Its regioselective iodine enables high-precision introduction of radioisotopes, resulting in diagnostic agents with high radiochemical purity and stability, demanded by global laboratory protocols.

    Industry compliance standards

    • ISO 13485:2016 for medical devices (including in vitro diagnostics)
    • FDA 21 CFR Part 820 for quality system regulation
    • European Pharmacopoeia monographs for radiolabeled compounds
    • ANSI N43.2 Radiation Safety Standards for Handling Isotopes

    Typical usage ratio

    • Dependent on label application, typically 0.02–0.06 g per batch in preclinical and clinical diagnostic probe synthesis

    Downstream process integration

    • Material enters during the initial radioiodination or isotopic exchange step, often under controlled temperature and anhydrous conditions, forming the radiolabel backbone for subsequent purification and formulation

    Final product types

    • Iodine-125 or Iodine-131 labeled pyridine tracer compounds
    • PET and SPECT imaging reagents for biochemical assays
    • In vitro diagnostic markers for pharmaceutical R&D

    4. Synthesis of Specialty Fine Chemicals for Electronic Materials

    Producers of specialty fine chemicals for electronics fabrication rely on this compound during the construction of high-purity pyridine derivatives, essential for photoresist and semiconductor precursor manufacturing. Its controlled reactivity supports consistent batch reproducibility in advanced material applications where trace contaminants and impurity profiles have measurable impacts on device performance.

    Industry compliance standards

    • SEMI C1 Chemical Specifications for Semiconductor Materials
    • IEC 62474 Material Declaration for Electronic Industry
    • RoHS Directive (2011/65/EU) for hazardous substances
    • Corporate Supplier Quality Agreements for Electronics OEMs

    Typical usage ratio

    • Generally 0.08–0.14 mol per mol of target electronic precursor; precise adjustment based on required device-layer purity and customer-specific impurity tolerances

    Downstream process integration

    • Material loaded at the functionalization phase of organic electronic precursor manufacturing, often just before integration into advanced thin-film or etching process streams

    Final product types

    • Pyridine-based photoresist sensitizers
    • Etchant stabilizer intermediates
    • Semiconductor-grade fine chemical additives
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    Certification & Compliance
    More Introduction

    2-Iodo-3-Hydroxypyridine: Crafting Reliable Building Blocks for Forward-Thinking Chemistry

    From Synthetic Challenge to Manufacturing Assurance

    In the world of chemical production, every material begins as a proposition: will it contribute true value to the landscape of organic synthesis, pharmaceutical discovery, or advanced materials science? 2-Iodo-3-Hydroxypyridine turned up years ago as one of those molecules that people asked for once in a while, and now, because of persistent molecular design and the expanding demand for heterocyclic intermediates, it features regularly in orders for downstream chemistry. Our perspective, coming from hands-on manufacturing rather than trading or custom rebranding, gives a clear window into why those who work at the bench level care about access to a reliable source of this compound—and why a straightforward, honest supply chain anchors progress in this space.

    Understanding 2-Iodo-3-Hydroxypyridine

    2-Iodo-3-Hydroxypyridine marries two hard-to-handle functional groups—iodine and hydroxyl—on a single pyridine ring. Its positioning on the ring is no accident: the iodo substituent at the second position offers a leverage point for cross-coupling or functional group transformation (palladium-catalyzed Suzuki, Sonogashira, and Heck-type reactions are all fair game), while the hydroxyl at position 3 opens routes toward protected pyridines, ethers, or as a nucleophile for further ring elaboration. The chemistries accessing these functions are both robust and sensitive; inconsistent quality hampers not only the yield but also the downstream process clean-up. We make it our job to ensure the features and quirks of this molecule arrive as expected every time.

    Why Purity and Traceability Matter

    Every kilo and every gram that leaves our loading dock tells a story of process control. In larger research centers and scale-up labs, the call for high-purity 2-Iodo-3-Hydroxypyridine remains unabated, especially as it moves into the pharmaceutical and agrochemical benches. This isn’t about chasing analytical perfection, but about minimizing batch failures and unrepeatable results. When a reaction veers off course (unexpected color, formation of gums, or rogue byproduct peaks by HPLC), there’s often one place to look first—the material’s provenance and how it was made, dried, and stored. We run multiple in-process quality checks, set rigorous moisture content boundaries, and move quickly to isolate and bottle so that shelf-life isn't compromised. Many have seen what happens if too much water, residual pyridine, or byproduct halide sneaks through: expensive errors downstream, and frustrated chemists who don’t want to troubleshoot their raw materials one bottle at a time.

    Model and Specifications Rooted in Practical Experience

    Our approach shuns haze and bureaucracy: we don’t go around tagging everything with convoluted product model numbers. Instead, we focus on what clients care about—analytical data that match real chemical expectations and direct customer feedback. Typical specifications are anchored in recommendations from pharmaceutical clients and reference literature: purity by HPLC above 98%, water content below 0.5%, and standard appearance checks. Samples from every lot go through NMR and mass spectrometry confirmation. Some clients want additional trace metal data if the final product lands in highly regulated applications; our process development team is set up to provide these when genuinely needed. And because storage and handling can impact long-term viability, we package this intermediate in dark HDPE jugs or glass, with inert gas overlays for larger drums, not out of formality but because we’ve lived the pain of cleaning up oxidized or decomposed stock.

    Streamlining the Synthetic Journey

    The principal value of 2-Iodo-3-Hydroxypyridine springs from its role as a junction in multi-step synthesis. The iodine atom serves as an exit ramp for broad coupling chemistry, making it ideal for sp^2–sp^2 or sp^2–sp^3 bond formation in biaryl or diaryl ethers, nitrogen-containing drugs, and experimental material science compounds. Colleagues in medicinal chemistry comment regularly about the speed-up in lead generation or library expansion when they start with high-quality, functionally diverse intermediates like this. The hydroxyl group at the 3-position enables regioselective functionalization—a benefit seen in both early discovery and process scale-up.

    Alternative methods to synthesize comparable derivatives tend to be less efficient, more prone to side reactions, or introduce hard-to-remove impurities. Fewer steps in the early stage means a cleaner chemical record, fewer variables in temperature swings or solvent residues, and more predictable success during scale-up. The cost of building a robust route using poorly defined intermediates stacks up quickly in lost time and wasted raw materials. Years of direct interaction with scale-up technicians and QC teams have taught us to prioritize what matters: consistency from ton-scale output down to custom sample batches.

    Comparisons to Other Pyridine Derivatives

    We routinely engage with customers who debate between using 2-Iodo-3-Hydroxypyridine and other iodinated or hydroxy-substituted pyridines. The landscape includes versions like 2-Iodo-4-Hydroxypyridine, 3-Iodo-2-Hydroxypyridine, and simpler hydroxy- or iodo-pyridines lacking the combination of both groups. Structurally, minor shifts in substitution pattern yield dramatic changes in chemical behavior. In practice, 2-Iodo-3-Hydroxypyridine often grants a more direct route to electron-rich cross-coupling targets due to enhanced reactivity of the ortho-iodo bond and the directing effects of the adjacent hydroxyl. We also see fewer issues with undesired side reactions compared to para-substituted analogues, especially in metal-catalyzed steps.

    From a manufacturing vantage, some analogues pose purification problems or lack batch stability; 2-Iodo-3-Hydroxypyridine, by contrast, carries a balanced profile: chemically active, easy to weigh and transfer, and typically less moisture sensitive than free aminopyridines or analogous halides. Analytical data support this: past lots tested after six months in unopened packaging have retained specified purity and no measurable decomposition under recommended storage conditions. Avoiding ambiguous or rare impurities stemming from mixed isomer formation gives further peace of mind during analytical validation or GMP process runs.

    Meeting the Evolving Needs of Industry

    As the pharmaceutical sector tightens its focus on reliability and traceability in the supply of core starting materials, small-molecule manufacturers are held to high practical standards—standards that often outstrip what specialty chemical traders observe. Our manufacturing runs target not just the stated analytical purity but also repeatability: the ability to restock a customer’s supply chain without unexpected delays, price shocks, or quality differences from lot to lot. Years in the business have shown us that web-based suppliers or offshore brokers sometimes oversell the generality of their offerings; direct conversations with clients clarify requirements and avoid confusion about regulatory paperwork, packaging requests, and special documentation.

    Some customers operate under pressure to minimize nitrosamine and residual solvent risks, especially since regulatory authorities have started tightening tolerance limits. Cross-contamination during multipurpose batch manufacturing can lead to stoppages and recalls. We separate flows to prevent issues; dedicated equipment avoids the nightmare of mysterious byproducts turning up in final product release tests. Our clients’ QA teams appreciate the extra mile—transparent batch records, open communication about lot composition, and readiness to field questions when audits come up. This transparency, rather than a regulatory checkbox, keeps the industrial process both honest and future-proof.

    Safety and Sustainability: Never Mere Afterthoughts

    Every batch of 2-Iodo-3-Hydroxypyridine requires careful stewardship from raw material intake to finished product. We source iodine from well-screened suppliers to prevent heavy metal contamination, and we handle all halogenated byproducts with due care—neutralization, solvent recovery, and post-reaction workup under controlled conditions. Waste minimization becomes especially important with molecules like this, given the persistence of halogens and the environmental impact if not recovered or detoxified properly.

    A lot of fine chemical operations pay only lip service to “green chemistry.” For us, targeted improvements actually grew out of necessity rather than ideology. For example, we implemented in-line monitoring of effluent to catch trace iodides and pyridine leachates long before compulsory local regulation. We recycle solvents, distill aqueous waste to allow reuse in preliminary cleaning, and batch-wash glassware to limit detergent run-off. Our on-site team tracks process metrics—kilograms of iodine consumed to output, yield per kilo of solvent, and overall mass balance per batch run—to identify ways to shrink the company’s environmental footprint. These habits, driven by hands-on problem-solving, connect directly to reducing batch costs and regulatory headaches rather than chasing sustainability “hot words” for marketing.

    Navigating Production and Scalability

    Producing 2-Iodo-3-Hydroxypyridine at scale, especially for pharmaceutical routes, is rarely routine. Certain reagents must be handled at low temperature or diluted under inert atmosphere to suppress side reactions. The hydroxyl group can create challenges with excessive byproduct solvation, risking yield loss if separation isn’t handled promptly. This means careful balancing of reaction kinetics, solvent choices, and purification steps—lessons we’ve internalized through years of optimization and by digging out of failed pilot runs or subpar recovery rates. Scale brings its own headaches: crystallization that worked on a 10 g scale may gum up at 5 kg; mixing that looked fine in a beaker generates hotspots and decomposition at 200 L. Rigorous scale-up trials and the willingness to discard batches that fall short help us maintain both margin and reputation.

    Pre-packaged catalogs rarely capture the true complexity involved. “Off-the-shelf” only describes stock that’s ready, not the labor and vigilance that smooths the flow from initial synthesis through multi-stage purification and careful, airtight storage. Our staff—chemi-operators, technicians, logistics experts—know that a late or low-quality delivery causes headaches across our customers’ time lines and budgets. Over time, open feedback loops and site visits to customer operations have sharpened our sensitivity to production challenges on both sides of the transaction. This shared outlook supports innovation without introducing avoidable process risk.

    Customer-Centered Adaptation and Problem Solving

    While the broader market for specialized pyridine intermediates grows ever more commoditized, longstanding, direct manufacturer-to-user relationships make a difference in the development of new synthetic targets. We’ve worked with pharma and biotech groups seeking ever-larger or sometimes uniquely purified lots for SAR (structure–activity relationship) studies and GMP route development. Our operators can tweak process parameters to push toward higher or lower moisture, normalize color, or minimize trace side products, all based on direct conversations rather than secondhand clearinghouses. Whether it’s single-digit gram runs or half-ton campaign manufacturing, this adaptability comes from firsthand problem solving, not from procedural checklists or standard operating manuals written for another continent’s regulatory regime.

    Few suppliers invite clients for on-site sampling or run tailored, small-scale validation batches ahead of production, but this hands-on process has prevented countless expensive surprises for both parties. A good portion of our process tweaks—switching filtration aids, adjusting crystallization solvent polarity, or optimizing drying times—arose from lab visits and mid-campaign feedback rather than any generic “continuous improvement plan.” This cross-pollination between supplier and user lets us track changing analytical or regulatory standards and address them directly, without lag or obfuscation. There’s satisfaction and a degree of pride in being able to sort technical snags in real time, before they become bottlenecks.

    Facing Tomorrow’s Challenges Together

    As regulatory stringency increases and timelines shrink—especially in clinical or pilot plant environments—direct manufacturers play a pivotal role in the new-product pipeline. No chemistry team wants to halt or rework a campaign because their base materials fall short. By focusing on practical support, traceability, and rigorous process control, we anchor progress for researchers and formulators alike. The ultimate benefit isn’t measured only in purity figures or analytical reports, but in repeatable, unexciting batch releases that let chemists write up successful experiments and process engineers plan runs with confidence.

    The ongoing evolution of medicinal chemistry strategies—coupling more complex heterocycles, building libraries faster, and running parallel syntheses—drives demand for flexible intermediate supply. Here, the distinct properties of 2-Iodo-3-Hydroxypyridine make it a cornerstone, not just another check-box on a reagent list. Its dual functional groups position it at the crossroad of multiple emerging synthetic approaches—fragment-based discovery, late-stage diversification, and “direct-to-biology” screening. We follow these trends closely by partnering directly with research clients and keeping an ear out for changes in process preferences and analytical needs.

    Final Thoughts From the Manufacturing Floor

    Years of hands-on production and technical support have solidified a simple conviction: success in chemical supply depends as much on operational integrity and collaborative feedback as technical know-how. With every order fulfilled, every batch tracked, and each new client interaction, we reaffirm our commitment to meet the demands of tomorrow’s labs and discovery teams. 2-Iodo-3-Hydroxypyridine stands as both a daily workhorse and a launchpad for new synthetic challenges. Customers deserve better than ambiguity or luck-of-the-draw intermediates. Reliability, transparency, and an open line between manufacturer and user make this possible—qualities that stem not from marketing, but from the grind and discipline of true chemical manufacturing.